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   <subfield code="a">Electrochemical investigation of a glassy carbon electrode modified with carbon nanotubes decorated with (poly)crystalline gold</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Antonio Radoi, Simona-Carmen Litescu, Sandra Eremia, Mihaela Miu, Mihai Danila, Adrian Dinescu, Gabriel-Lucian Radu]</subfield>
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   <subfield code="a">Multiwalled carbon nanotubes with nanosized sputtered gold were used to modify a glassy carbon electrode (GCE). The substrate was characterized by scanning electron microscopy (SEM), X-ray diffraction, cyclic voltammetry and amperometry. SEM micrographs indicated an uniform coverage of the carbon nanotubes with nanosized (poly)crystalline gold. Cyclic voltammetry reveals that peak separation of the unmodified GCE in the presence of 1mM ferricyanide is 131mV, but 60mV only for the modified GCE. In addition, the oxidation of NADH (1mmolL−1 solution) begins at negative potentials (around −100mV vs. Ag/AgCl), and the anodic peak potential (corresponding to the irreversible oxidation of NADH) is found at +94mV. The effect of pH on the electrocatalytic activity was studied in the range from 5.4 to 8.0. The relationship between the anodic peak potential and the pH indicated a variation of −33.5mV/pH which is in agreement with a two-electron and one-proton reaction mechanism. Amperometry, performed at either −50 or +50mV vs. an Ag/AgCl reference electrode, indicates that the modified electrode is a viable amperometric sensor for NADH. At a working potential of +50mV, the response to NADH is linear in the concentration range from 1 to 100μmolL−1, with an RSD of 6% (n = 4). Figure Multiwalled carbon nanotubes with nanosized sputtered gold were used to modify a glassy carbon electrode. The oxidation of NADH (1mmolL−1) begins at negative potentials (around −100mV vs. Ag/AgCl), and the anodic peak potential (corresponding to the irreversible oxidation of NADH) is found at +94mV.</subfield>
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